Canonical Allele Identifier: CA2123464995

Gene: MYH7 MHRT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23415992_23415993delinsCT , CM000676.2:g.23415992_23415993delinsCT	GRCh38
NC_000014.8:g.23885201_23885202delinsCT , CM000676.1:g.23885201_23885202delinsCT	GRCh37
NC_000014.7:g.22955041_22955042delinsCT	NCBI36
NG_007884.1:g.24669_24670delinsAG , LRG_384:g.24669_24670delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.4953+11_4953+12delinsAG (MYH7) MANE Select	ENSP00000347507.3:n.4953+11_4953+12delinsAG
ENST00000355349.3:c.4953+11_4953+12delinsAG (MYH7)	ENSP00000347507.3:n.4953+11_4953+12delinsAG
NM_000257.3:c.4953+11_4953+12delinsAG (MYH7)	NP_000248.2:n.4953+11_4953+12delinsAG
NR_126491.1:n.262-9_262-8delinsCT (MHRT)
XM_017021340.1:c.4953+11_4953+12delinsAG (MYH7)	XP_016876829.1:n.4953+11_4953+12delinsAG
NM_000257.4:c.4953+11_4953+12delinsAG (MYH7) MANE Select	NP_000248.2:n.4953+11_4953+12delinsAG